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ES2143238T3 - DERIVATIVES OF 1- (PIPERIDINIL SUBSTITUTED IN POSITIONS 1,2) -PIPERAZINES SUBSTITUTED IN POSITION 4. - Google Patents

DERIVATIVES OF 1- (PIPERIDINIL SUBSTITUTED IN POSITIONS 1,2) -PIPERAZINES SUBSTITUTED IN POSITION 4.

Info

Publication number
ES2143238T3
ES2143238T3 ES96937248T ES96937248T ES2143238T3 ES 2143238 T3 ES2143238 T3 ES 2143238T3 ES 96937248 T ES96937248 T ES 96937248T ES 96937248 T ES96937248 T ES 96937248T ES 2143238 T3 ES2143238 T3 ES 2143238T3
Authority
ES
Spain
Prior art keywords
het
alkyl
rent
substituted
formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
ES96937248T
Other languages
Spanish (es)
Inventor
Frans Eduard Janssens
Francois Maria Sommen
Dominique Louis Nest Surleraux
Joseph Elisabeth Leenaerts
Roosbroeck Yves Emiel Mari Van
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Janssen Pharmaceutica NV
Original Assignee
Janssen Pharmaceutica NV
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Filing date
Publication date
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=8220780&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ES2143238(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Janssen Pharmaceutica NV filed Critical Janssen Pharmaceutica NV
Application granted granted Critical
Publication of ES2143238T3 publication Critical patent/ES2143238T3/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P23/00Anaesthetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Hospice & Palliative Care (AREA)
  • Otolaryngology (AREA)
  • Anesthesiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

ESTA INVENCION SE RELACIONA CON COMPUESTOS DE FORMULA (I), LAS FORMAS N-OXIDO, LAS SALES DE ADICION FARMACEUTICAMENTE ACEPTABLES Y SUS FORMAS ESTEROISOMERICAS, EN LAS QUE N ES 0, 1 O 2; M ES 1 O 2, CON TAL QUE, SI M ES 2, ENTONCES N ES 1; P ES 1 O 2; = Q ES = O O = NR 3 ; X ES UN ENLACE COVALENTE O UN RADICAL BIVALENTE DE FORMULA O-, -S-, -NR 3 -; R 1 ES AR 1 , AR 1 , AR 1 C 1-6 ALQUILO O DI(AR 1 )C 1-6 ALQUILO, EN DONDE CADA GRUPO C 16 ALQUILO ES OPCIONALMENTE SUSTITUIDO CON HIDROXI, C 14 ALQUILOXI, OXO O UN SUBSTITUYENTE OXO CETALIZADO; R 2 ES AR 2 , AR SUP,1 C 1-6 ALQUILO, HET 1 O HET 1 C 1-6 ALQ UILO; R 3 ES HIDROGENO O UN ALQUILO C 1-6 ; L ES HIDROGENO; AR 3 ; C 1-6 ALQUILO; C 1-6 ALQUILO SUSTITU IDO CON 1 O 2 SUBSTITUYENTES SELECCIONADOS DE UN GRUPO DE HIDROXI, C 1-6 ALQUILOXI, AR 3 , AR 3 C 1-6 ALQUIL OXI Y HET 2 ; C 36 ALQUENILO; AR 3 C 3-6 ALQUENILO; DI(AR 3 )C 36 ALQUENILO O UN RADICAL DE FORMULA (A-1), (A-2), (A-3), (A-4) O (A-5); AR 1 , AR 2 , AR SUP,3 SON TODOS FENILO O FENILOSUSTITUIDO; HET 1 Y HET S UP,2 SON HETEROCICLOS MONOCICLICOS O BICICLICOS; ESTOS COMPUESTOS SON ANTAGONISTAS DE LA SUSTANCIA P; SE DESCRIBE SU PREPARACION, COMPOSICIONES QUE LOS CONTIENEN Y SU USO COMO MEDICAMENTOS.THIS INVENTION IS RELATED TO COMPOUNDS OF FORMULA (I), N-OXIDE FORMS, PHARMACEUTICALLY ACCEPTABLE ADDITIONAL SALTS AND THEIR STEROISOMERIC FORMS, IN WHICH N IS 0, 1 OR 2; M IS 1 OR 2, SO IF M IS 2, THEN N IS 1; P ES 1 O 2; = Q ES = O O = NR 3; X IS A COVALENT LINK OR A BIVALENT RADICAL OF FORMULA O-, -S-, -NR 3 -; R 1 IS AR 1, AR 1, AR 1 C 1-6 RENT OR DI (AR 1) C 1-6 RENT, WHERE EACH GROUP C 16 RENT IS OPTIONALLY SUBSTITUTED WITH HYDROXY, C 14 ALKYL OXY, OX OR A SUBSTITUTE OXO CETALLIZED; R 2 ES AR 2, AR SUP, 1 C 1-6 ALKYL, HET 1 OR HET 1 C 1-6 ALK UILO; R 3 IS HYDROGEN OR A C 1-6 ALKYL; L IS HYDROGEN; AR 3; C 1-6 RENT; C 1-6 ALKYL SUBSTITUTE IDO WITH 1 OR 2 SELECTED SUBSTITUTES FROM A GROUP OF HYDROXY, C 1-6 ALKYLLOX, AR 3, AR 3 C 1-6 ALKYL OXI AND HET 2; C 36 ALKYLENE; AR 3 C 3-6 ALKYNYLL; DI (AR 3) C 36 ALKYLLY OR A RADICAL OF FORMULA (A-1), (A-2), (A-3), (A-4) O (A-5); AR 1, AR 2, AR SUP, 3 ARE ALL PHENYL OR SUBSTITUTE PHENYL; HET 1 AND HET S UP, 2 ARE MONOCYCLE OR BICYCLE HETEROCICLES; THESE COMPOUNDS ARE ANTAGONISTS OF THE SUBSTANCE P; THEIR PREPARATION, COMPOSITIONS CONTAINING THEM AND THEIR USE AS MEDICINES ARE DESCRIBED.

ES96937248T 1995-10-30 1996-10-25 DERIVATIVES OF 1- (PIPERIDINIL SUBSTITUTED IN POSITIONS 1,2) -PIPERAZINES SUBSTITUTED IN POSITION 4. Expired - Lifetime ES2143238T3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP95202929 1995-10-30

Publications (1)

Publication Number Publication Date
ES2143238T3 true ES2143238T3 (en) 2000-05-01

Family

ID=8220780

Family Applications (1)

Application Number Title Priority Date Filing Date
ES96937248T Expired - Lifetime ES2143238T3 (en) 1995-10-30 1996-10-25 DERIVATIVES OF 1- (PIPERIDINIL SUBSTITUTED IN POSITIONS 1,2) -PIPERAZINES SUBSTITUTED IN POSITION 4.

Country Status (31)

Country Link
US (3) US6197772B1 (en)
EP (1) EP0862566B1 (en)
JP (1) JP3073238B2 (en)
KR (1) KR100407067B1 (en)
CN (2) CN100415716C (en)
AR (1) AR004698A1 (en)
AT (1) ATE188691T1 (en)
AU (1) AU704155B2 (en)
BR (1) BR9611184B8 (en)
CA (1) CA2234096C (en)
CY (1) CY2177B1 (en)
CZ (1) CZ291794B6 (en)
DE (1) DE69606196T2 (en)
DK (1) DK0862566T3 (en)
EA (1) EA000909B1 (en)
ES (1) ES2143238T3 (en)
GR (1) GR3033154T3 (en)
HR (1) HRP960507B1 (en)
HU (1) HU227341B1 (en)
IL (1) IL123962A (en)
MX (1) MX9803407A (en)
MY (1) MY116575A (en)
NO (1) NO310232B1 (en)
NZ (1) NZ321575A (en)
PL (1) PL185029B1 (en)
PT (1) PT862566E (en)
SI (1) SI0862566T1 (en)
TR (1) TR199800756T2 (en)
TW (1) TW460473B (en)
WO (1) WO1997016440A1 (en)
ZA (1) ZA969090B (en)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ321575A (en) * 1995-10-30 1999-05-28 Janssen Pharmaceutica Nv 1-(1,2-disubstituted piperidinyl)-4- substituted piperazine derivatives
TW382017B (en) 1995-12-27 2000-02-11 Janssen Pharmaceutica Nv 1-(1,2-disubstituted piperidinyl)-4-(fused imidazole)-piperidine derivatives
TW429256B (en) * 1995-12-27 2001-04-11 Janssen Pharmaceutica Nv 1-(1,2-disubstituted piperidinyl)-4-(benzimidazolyl- and imidazopyridinyl)-piperidine derivatives
TW531537B (en) 1995-12-27 2003-05-11 Janssen Pharmaceutica Nv 1-(1,2-disubstituted piperidinyl)-4-substituted piperidine derivatives
AU2307899A (en) * 1997-12-23 1999-07-12 Alcon Laboratories, Inc. Muscarinic agents and use thereof to treat glaucoma, myopia and various other conditions
US6689765B2 (en) 1999-05-04 2004-02-10 Schering Corporation Piperazine derivatives useful as CCR5 antagonists
US6391865B1 (en) 1999-05-04 2002-05-21 Schering Corporation Piperazine derivatives useful as CCR5 antagonists
USRE39921E1 (en) 1999-10-07 2007-11-13 Smithkline Beecham Corporation Chemical compounds
GB9923748D0 (en) 1999-10-07 1999-12-08 Glaxo Group Ltd Chemical compounds
WO2001030348A1 (en) * 1999-10-25 2001-05-03 Janssen Pharmaceutica N.V. Use of substance p antagonists for influencing the circadian timing system
GB0025354D0 (en) * 2000-10-17 2000-11-29 Glaxo Group Ltd Chemical compounds
ES2342942T3 (en) 2001-03-29 2010-07-19 Schering Corporation CCR5 ANTAGONISTS USEFUL FOR THE TREATMENT OF AIDS.
GB0108594D0 (en) * 2001-04-05 2001-05-23 Glaxo Group Ltd Chemical compounds
GB0203022D0 (en) 2002-02-08 2002-03-27 Glaxo Group Ltd Chemical compounds
WO2003066589A1 (en) * 2002-02-08 2003-08-14 Glaxo Group Limited Piperidylcarboxamide derivatives and their use in the treatment of tachykinim-mediated diseases
GB0203020D0 (en) * 2002-02-08 2002-03-27 Glaxo Group Ltd Chemical compounds
CA2487141C (en) 2002-06-24 2011-08-02 Janssen Pharmaceutica N.V. Process for the production of n-(2,6-dimethyl-phenyl)-2-piperazin-1-yl-acetamide
UA81918C2 (en) * 2002-10-08 2008-02-25 Янссен Фармацевтика Н.В. Normal;heading 1;heading 2;SUBSTITUTED 1,4-DI-PIPERIDIN-4-YL-PIPERAZINE DERIVATIVES AND THEIR USE AS NEUROKININ ANTAGONISTS
WO2004056772A1 (en) * 2002-12-23 2004-07-08 Janssen Pharmaceutica N.V. Substituted 1,4-di-piperidin-4-yl-piperazine derivatives and their use as tachykinin antagonists
MY141736A (en) * 2002-10-08 2010-06-15 Elanco Animal Health Ireland Substituted 1,4-di-piperidin-4-yi-piperazine derivatives and their use as neurokinin antagonists
US7582761B2 (en) * 2002-10-17 2009-09-01 Amgen Inc. Vanilloid receptor ligands and their use in treatments
JO2485B1 (en) * 2002-12-23 2009-01-20 شركة جانسين فارماسوتيكا ان. في Substituted 1- Piperidin- 3- Yl- 4- Piperidin- 4- Yl- Piperazine Derivatives and their Use as Neurokinin Antagonists
EP1578744B1 (en) 2002-12-23 2008-07-09 Janssen Pharmaceutica N.V. Substituted 4-(4-piperidin-4-yl-piperazin-1-yl)-azepane derivatives and their use as neurokinin antagonists
JO2696B1 (en) 2002-12-23 2013-03-03 شركة جانسين فارماسوتيكا ان. في Substituted 1-piperidin-4-yl-4-pyrrolidin-3-yl-piperazine derivatives and their use as neurokinin antagonists
JP4660199B2 (en) 2002-12-23 2011-03-30 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ Substituted 1-piperidin-4-yl-4-azetidin-3-yl-piperazine derivatives and their use as neurokinin antagonists
DE602004013772D1 (en) * 2003-06-10 2008-06-26 Janssen Pharmaceutica Nv Combination of opioids and a piperazine derivative for the treatment of pain
JP2006527236A (en) * 2003-06-10 2006-11-30 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ Substituted 1,4-di-piperidin-4-yl-piperazine derivatives in combination with opioid analgesics and their use for the treatment of pain and side effects associated with opioid based treatments
UY28538A1 (en) * 2003-09-26 2005-04-29 Vertex Pharma PHENYL-PIPERAZINE DERIVATIVES AS MUSCARINIC RECEPTORS MODULATORS
JO2676B1 (en) * 2004-04-06 2012-06-17 جانسين فارماسوتيكا ان. في Substituted diaza-spiro-(4,5)-Decane derivatives and their use as neurokinin antagonists
JO2527B1 (en) * 2004-04-06 2010-03-17 شركة جانسين فارماسوتيكا ان. في Substiuted diaza-spiro-(5,5)-Deacan derivatives and there use as neurokinin antagonist
JO2525B1 (en) * 2004-04-08 2010-03-17 شركة جانسين فارماسوتيكا ان. في Substiuted 4-alkyl-and 4-alkanoyl piperidine derivatives and there use as neurokinin antagonist
ES2431524T3 (en) 2004-04-13 2013-11-26 Incyte Corporation Piperazinylpiperidine derivatives as chemokine receptor antagonists
WO2005123081A2 (en) * 2004-06-22 2005-12-29 Janssen Pharmaceutica N.V. (2-benzyl-4-{4-[1-(tetrahydrofuran-3-carbonyl)-pyrrolidin-3-yl]-piperazin-1-yl}-piperidin-1-yl)-(3,5-trifluoromethyl-phenyl))-methanone for the treatment of schizophrenia
US20060024481A1 (en) * 2004-07-29 2006-02-02 Eastman Kodak Company Jet printing of patterned metal
CA2576166C (en) 2004-08-19 2018-02-20 Monsanto Technology Llc Glyphosate salt herbicidal composition
WO2006071958A1 (en) * 2004-12-29 2006-07-06 Millennium Pharmaceuticals, Inc. Compounds useful as chemokine receptor antagonists
NZ556628A (en) 2005-03-08 2009-09-25 Janssen Pharmaceutica Nv Diaza-spiro-[4.4]-nonane derivatives as neurokinin (NK1) antagonists
CN101190330A (en) 2006-11-30 2008-06-04 深圳市鼎兴生物医药技术开发有限公司 Application of cholinesterase in antagonizing tachykinin drugs
WO2008090114A1 (en) 2007-01-24 2008-07-31 Glaxo Group Limited Pharmaceutical compositions comprising 2-methoxy-5- (5-trifluoromethyl-tetrazol-i-yl-benzyl) - (2s-phenyl-piperidin-3s-yl-)
WO2010081851A1 (en) 2009-01-14 2010-07-22 Genoscience Pharma Piperidin-4-ylpiperazine compounds for the treatment of hcv infection
GB201106817D0 (en) 2011-04-21 2011-06-01 Astex Therapeutics Ltd New compound
GB201218850D0 (en) 2012-10-19 2012-12-05 Astex Therapeutics Ltd Bicyclic heterocycle compounds and their uses in therapy
GB201218864D0 (en) 2012-10-19 2012-12-05 Astex Therapeutics Ltd Bicyclic heterocycle compounds and their uses in therapy
US9980973B2 (en) 2012-10-19 2018-05-29 Astex Therapeutics Limited Bicyclic heterocycle compounds and their uses in therapy
GB201218862D0 (en) 2012-10-19 2012-12-05 Astex Therapeutics Ltd Bicyclic heterocycle compounds and their uses in therapy
CN111557432B (en) 2013-02-08 2023-08-04 通用磨坊公司 Low sodium food
LT3083616T (en) 2013-12-20 2021-09-10 Astex Therapeutics Limited BICYCLIC HETEROCYCL COMPOUNDS AND THEIR USE IN THERAPY
MX371178B (en) * 2016-01-08 2020-01-21 Nerre Therapeutics Ltd ORVEPITANT FOR THE TREATMENT OF CHRONIC COUGH.

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2676055B1 (en) * 1991-05-03 1993-09-03 Sanofi Elf AMINO POLYCYCLIC COMPOUNDS AND THEIR ENANTIOMERS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM.
MY110227A (en) * 1991-08-12 1998-03-31 Ciba Geigy Ag 1-acylpiperindine compounds.
CN1042335C (en) * 1993-01-03 1999-03-03 诺瓦提斯公司 1-acylpiperidine compounds
ATE157349T1 (en) * 1993-05-12 1997-09-15 Heumann Pharma Gmbh & Co STABLE AND CRYSTALLINE FORM OF BEZAFIBRATE
GB9310066D0 (en) * 1993-05-17 1993-06-30 Zeneca Ltd Alkyl substituted heterocycles
WO1995011895A1 (en) * 1993-10-26 1995-05-04 Ciba-Geigy Ag N-benzoyl-4-oxy/thio-2-substituted piperidines as substance-p receptor antagonists
IL111730A (en) * 1993-11-29 1998-12-06 Fujisawa Pharmaceutical Co Piperazine derivatives processes for the preparation thereof and pharmaceutical compositions containing the same
KR100254666B1 (en) * 1994-07-15 2000-05-01 이치로 키타사토 Novel compounds with platelet aggregation inhibitory action
CA2198382A1 (en) * 1994-09-30 1996-04-11 Novartis Ag 1-acyl-4-aliphatylaminopiperidine compounds
NZ321575A (en) * 1995-10-30 1999-05-28 Janssen Pharmaceutica Nv 1-(1,2-disubstituted piperidinyl)-4- substituted piperazine derivatives

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